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Axenfeld-Rieger syndrome type 2 (DOID:0110121)
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Parent Terms Term With Siblings Child Terms
anodontia +     
Maxillary Diseases +     
ADULT syndrome  
Aloi Tomasini Isaia Syndrome 
Anodontia of Permanent Dentition 
Axenfeld-Rieger Anomaly with Cardiac Defects and Sensorineural Hearing Loss 
Axenfeld-Rieger syndrome type 1  
Axenfeld-Rieger syndrome type 2 
An Axenfeld-Rieger syndrome that has_material_basis_in deletions in the region 13q14. (DO)
Axenfeld-Rieger syndrome type 3  
Cleft Palate, Deafness, and Oligodontia 
Deafness Oligodontia Syndrome 
Dermatoosteolysis Kirghizian Type 
Dilated Cardiomyopathy with Woolly Hair, Keratoderma, and Tooth Agenesis  
Dysmyelinating Leukodystrophy with Oligodontia 
Ectodermal Dysplasia, Trichoodontoonychial Type 
Growth Retardation, Alopecia, Pseudoanodontia and Optic Atrophy  
Hypodontia Oligodontia with Orofacial Cleft 
hypohidrotic ectodermal dysplasia +   
hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism  
Late-Onset Localized Junctional Epidermolysis Bullosa with Mental Retardation 
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
Maxillary Neoplasms +   
Mehta Lewis Patton Syndrome 
Microdontia Hypodontia Short Stature 
Oligodontia-Colorectal Cancer Syndrome  
Pinheiro Freire-Maia Miranda Syndrome 
Schopf-Schulz-Passarge syndrome  
solitary median maxillary central incisor  
Split-Hand and Split-Foot With Hypodontia 
Taurodontia Absent Teeth Sparse Hair 
Thai Symphalangism Syndrome 
Thumb Deformity, Alopecia, Pigmentation Anomaly 
tooth and nail syndrome  
X-Linked Hypodontia 
Zadik Barak Levin Syndrome 

Exact Synonyms: RIEG2 ;   Rieger syndrome 2 ;   Rieger syndrome type 2
Primary IDs: MESH:C535680
Alternate IDs: OMIM:601499 ;   RDO:0000935 ;   RDO:0008820
Xrefs: ICD10CM:Q13.8
Definition Sources:

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.